Canonical Allele Identifier: CA1327322051
Gene: ATIC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.215325204C= , CM000664.2:g.215325204C= GRCh38
NC_000002.11:g.216189927C= , CM000664.1:g.216189927C= GRCh37
NC_000002.10:g.215898172C= NCBI36
NG_013002.1:g.18249C=

Transcript Alleles

HGVS Amino-acid change
ENST00000236959.14:c.291-37C= MANE Select ENSP00000236959.9:n.291-37C=
ENST00000236959.13:c.291-37C= ENSP00000236959.9:n.291-37C=
ENST00000413174.1:c.114-37C= ENSP00000402393.1:n.114-37C=
ENST00000427397.5:c.*341-37C= ENSP00000394317.1:n.*341-37C=
ENST00000435675.5:c.288-37C= ENSP00000415935.1:n.288-37C=
ENST00000443953.5:c.*388-37C= ENSP00000406792.1:n.*388-37C=
ENST00000444305.5:c.224-37C= ENSP00000388675.1:n.224-37C=
ENST00000488712.5:n.466C=
NM_004044.6:c.291-37C= NP_004035.2:n.291-37C=
XM_017004187.2:c.291-37C= XP_016859676.1:n.291-37C=
XM_024452919.1:c.114-37C= XP_024308687.1:n.114-37C=
NM_004044.7:c.291-37C= MANE Select NP_004035.2:n.291-37C=